Skip to Content
MilliporeSigma
All Photos(3)

Documents

F2003

Sigma-Aldrich

Flavone

≥99.0%

Synonym(s):

2-Phenyl-4H-1-benzopyran-4-one, 2-Phenylchromone

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Empirical Formula (Hill Notation):
C15H10O2
CAS Number:
525-82-6
Molecular Weight:
222.24
Beilstein/REAXYS Number:
157598
EC Number:
208-383-8
MDL number:
MFCD00006825
UNSPSC Code:
12352100
PubChem Substance ID:
57654180
NACRES:
NA.22

assay

≥99.0%

form

powder

mp

94-97 °C (lit.)

SMILES string

O=C1C=C(Oc2ccccc12)c3ccccc3

InChI

1S/C15H10O2/c16-13-10-15(11-6-2-1-3-7-11)17-14-9-5-4-8-12(13)14/h1-10H

InChI key

VHBFFQKBGNRLFZ-UHFFFAOYSA-N

Gene Information

human ... ADORA3(140) , ANPEP(290) , CYP1A2(1544)
mouse ... Hexa(15211)
rat ... Adora1(29290) , Adora2a(25369) , Ar(24208) , Gabra2(29706)

Looking for similar products? Visit Product Comparison Guide

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

trans-Chalcone 97%

Sigma-Aldrich

136123

trans-Chalcone

Aaron Ciechanover et al.
Experimental & molecular medicine, 47, e147-e147 (2015-03-15)
Mammalian cells remove misfolded proteins using various proteolytic systems, including the ubiquitin (Ub)-proteasome system (UPS), chaperone mediated autophagy (CMA) and macroautophagy. The majority of misfolded proteins are degraded by the UPS, in which Ub-conjugated substrates are deubiquitinated, unfolded and cleaved
León Jesús German-Ponciano et al.
Neurochemistry international, 140, 104850-104850 (2020-09-23)
Chrysin (5,7-dihydroxyflavone), a nutraceutical flavonoid present in diverse plants, has a backbone structure shared with the flavone backbone, with additional hydroxyl groups that confers its antioxidant properties and effects at the GABAA receptor complex. However, whether these effects are due
Daria Nitarska et al.
BMC plant biology, 18(1), 216-216 (2018-10-05)
Commercially available poinsettia (Euphorbia pulcherrima) varieties prevalently accumulate cyanidin derivatives and show intense red coloration. Orange-red bract color is less common. We investigated four cultivars displaying four different red hues with respect to selected enzymes and genes of the anthocyanin
Yu-Wan Ni et al.
Plants (Basel, Switzerland), 9(5) (2020-05-21)
Functional constituents in the leaves of Passiflora plants contain antidepressant and antianxiety effects which are beneficial to human health and fitness. The objective of this study was to investigate leaf growth, physiological parameters, and secondary metabolite contents of Tainung No.
Tanya Welgemoed et al.
Frontiers in plant science, 11, 191-191 (2020-04-02)
Gray leaf spot (GLS) disease in maize, caused by the fungus Cercospora zeina, is a threat to maize production globally. Understanding the molecular basis for quantitative resistance to GLS is therefore important for food security. We developed a de novo
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service